watchara boonsawat

Prof. watchara boonsawat

Khon Kaen University, Khon Kaen, Thailand
orcid

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2003 in Respiratory Medicine
Verified
Journal Article
Closed access
WBwatchara boonsawat
watchara boonsawat
SCS Charoenratanakul
S Charoenratanakul
CPChaicharn Pothirat
Chaicharn Pothirat
KSK Sawanyawisuth
K Sawanyawisuth
TST Seearamroongruang
T Seearamroongruang
OSO Selroos
O Selroos

1 August 2004 in Respirology
Verified
Journal Article
Closed access
PDF file
WBwatchara boonsawat
watchara boonsawat
PCPoonkasem Charoenphan
Poonkasem Charoenphan
SKSumalee Kiatboonsri
Sumalee Kiatboonsri
SWSomkiat Wongtim
Somkiat Wongtim
VVVilaiwan Viriyachaiyo
Vilaiwan Viriyachaiyo
NTNikom Thanomsieng
Nikom Thanomsieng

PPPum Phusahat
Pum Phusahat
Piyameth DilokthornsakulPiyameth Dilokthornsakul
Piyameth Dilokthornsakul
WBwatchara boonsawat
watchara boonsawat
UZUraiwan Zaeoue
Uraiwan Zaeoue
NHNadthatida Hansuri
Nadthatida Hansuri
SSunee Lertsinudom
Sunee Lertsinudom
Background: Cytisine is a prospective pharmacological alternative for community pharmacy smoking cessation services. However, it has not yet been licensed because of a lack of efficacy and safety information in Thailand. Objective: The aim of this study was to evaluate the efficacy of cytisine in combination with community pharmacists’ counselling on smoking cessation in a community pharmacy in ThailandDesign. Setting, participants, and interventions: A double-blinded randomized placebo-controlled trials was carried out. Participants aged >18 years old who smoked >10 tobaccos/day were randomly assigned to receive cytisine or placebo and five sessions of counselling by a community pharmacist. The primary outcome was a continuous abstinence rate (CAR) at week 48. The CAR was also measured at weeks 2, 4, 12, and 24. Adverse events were monitored. Results: A total of 132 participants were included, with 67 receiving cytisine and 65 receiving a placebo. Approximately 95% of participants were male. The CARs were determined to be 14.93% and 6.15% for cytisine and placebo, respectively, at week 48. The relative risk (RR) was 2.41 (95% confidence interval (CI); 0.80–7.35, p = 0.102). The RRs for CAR at weeks 2, 4, 12, and 24 were 2.43, 2.91, 2.50, and 1.78, respectively. Only the RRs for weeks 2, 4, and 12 were statistically significant. Common and non-serious gastrointestinal and neurological adverse events were observed. Conclusion: Cytisine, when combined with community pharmacists’ counselling, did not statistically improve the CAR at week 48, although it did improve the CAR at weeks 2, 4, and 12. Adverse events of cytisine were common and non-serious (registration number: TCTR20180312001).

KWKampanat Wangsan
Kampanat Wangsan
NCNaesinee Chaiear
Naesinee Chaiear
KSKittisak Sawanyawisuth
Kittisak Sawanyawisuth
PKPiyanee Klainin-Yobas
Piyanee Klainin-Yobas
KSKanjana Simajareuk
Kanjana Simajareuk
WBwatchara boonsawat
watchara boonsawat
Shiftwork is related to an increased risk of several diseases, including gastric ulcers, myocardial infarction, and diabetes. Several shiftwork patterns are related to poor sleep quality, such as a quick returns or extended shifts. This study aimed to find the shiftwork patterns strongly associated with poor sleep quality amongst nurses. A cross-sectional analytical study was conducted among nurses working for at least one month. The sub-groups were the good sleep quality group (n = 150) and the poor sleep quality group (n = 472). Eligible participants were asked to complete a self-reported questionnaire comprising personal characteristics, job characteristics, shiftwork characteristics, and sleep quality. Factors associated with poor sleep quality were determined using logistic regression analysis. Two factors associated with poor sleep quality remained in the final model: viz., depression and backward rotational shift. The only independent factor for poor sleep quality was a backward rotational shift with an adjusted odds ratio (95% CI) of 1.946 (1.344, 2.871). In conclusion, compared with other shift patterns, backward shiftwork was the most significant factor associated with poor sleep quality and should be avoided.

1 January 2008 in Clinical Drug Investigation
Verified
Journal Article
Closed access
PDF file
WBwatchara boonsawat
watchara boonsawat
LGLudmila Goryachkina
Ludmila Goryachkina
LJLoretta Jacques
Loretta Jacques
LFLucy Frith
Lucy Frith

28 May 2025 in Respiratory Medicine
Verified
Journal Article
Open access
NHNicola A. Hanania
Nicola A. Hanania
RSRichard Stanford
Richard Stanford
ARAdrián Rendón
Adrián Rendón
BGBilun Gemicioglu
Bilun Gemicioglu
LFLeandro Fritscher
Leandro Fritscher
MHMohamed Hamouda
Mohamed Hamouda
Asthma affects over 260 million people globally, with significant health impacts. The Global Initiative for Asthma (GINA) 2024 report recommends inhaled corticosteroid/long-acting β2-agonist (ICS/LABA) combinations, including fluticasone propionate/salmeterol (FP/SAL) and budesonide/formoterol (BUD/FOR), for maintenance treatment. Both combinations have demonstrated clinical benefits, with previous clinical trials and real-world studies showing comparable asthma control with FP/SAL and BUD/FOR. This United States (US)-based study compares the real-world effectiveness of FP/SAL and BUD/FOR on asthma control and treatment adherence. This retrospective cohort study analyzed data from the US Optum's Market Clarity database (July 1, 2010, to December 31, 2019), with integrated medical, pharmacy claims, and clinical electronic health records. Patients aged ≥18 years with asthma at GINA Steps 3-4, and ≥1 pharmacy claim for FP/SAL or BUD/FOR (index) were included. Patients on other ICS/LABA therapy ≥12 months prior to index were excluded. Inverse probability of treatment weighting adjusted for confounders. Outcomes were stratified by asthma severity. A total of 57,000 patients were included (FP/SAL: 28,639; BUD/FOR: 28,361). Baseline characteristics were balanced post-weighting. Asthma control was similar between cohorts, with no significant differences in Asthma Control Test scores or short-acting β2-agonist fills during the 12-month period following the index. Treatment adherence, assessed using proportion of days covered (≥0.8), was higher in the FP/SAL cohort (5.4 %) versus the BUD/FOR cohort (4.4 %; p < 0.001). FP/SAL and BUD/FOR were similarly effective for asthma control in real-world settings, while FP/SAL was generally associated with greater medication adherence, a key factor for long-term control.